Screening for creatine transporter deficiency in autism spectrum disorder: a pilot study von Arslan, Mutluay, Yildiz, Yılmaz, Olgaç, Asburçe, Hekim, Özlem, Yücel, Çiğdem, Sertoğlu, Erdim

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Can serum orexin levels be used as a marker in childhood epilepsy? von Arslan, Mutluay, Üstün, Canan, Coşkun, Ayşe Nur, Çelik, Hasan, Yalçın, Hacı Nadir, Karaismailoğlu, Eda, Sertoğlu, Erdim, Ünay, Bülent

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A Rare Cause of Hyperinsulinemic Hypoglycemia: Kabuki Syndrome von Mısırlıgil, Mina, Yıldız, Yılmaz, Akın, Onur, Odabaşı Güneş, Sevinç, Arslan, Mutluay, Ünay, Bülent

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Clinical Heterogeneity in MT-ATP6 Pathogenic Variants: Same Genotype-Different Onset von Capiau, Sara, Smet, Joél, De Paepe, Boel, Yildiz, Yilmaz, Arslan, Mutluay, Stevens, Olivier, Verschoore, Maxime, Stepman, Hedwig, Seneca, Sara, Vanlander, Arnaud

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Evaluation of Plasma Melatonin Levels in Children With Afebrile and Febrile Seizures von Dabak, Orçun, MD, Altun, Demet, MD, Arslan, Mutluay, MD, Yaman, Halil, MD, Vurucu, Sabahattin, MD, Yesilkaya, Ediz, MD, Unay, Bulent, MD

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Association of neck circumference and pulmonary function in children von Akın, Onur, MD, Arslan, Mutluay, MD, Haymana, Cem, MD, Karabulut, Erdem, PhD, Hacihamdioglu, Bulent, MD, Yavuz, Suleyman Tolga, MD

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Association of wider neck circumference and asthma in obese children von Akın, Onur, MD, Sarı, Erkan, MD, Arslan, Mutluay, MD, Yeşilkaya, Ediz, MD, Hacihamdioglu, Bulent, MD, Yavuz, Suleyman Tolga, MD

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Visual and brainstem auditory evoked potentials in children with obesity von Akın, Onur, Arslan, Mutluay, Akgün, Hakan, Yavuz, Süleyman Tolga, Sarı, Erkan, Taşçılar, Mehmet Emre, Ulaş, Ümit Hıdır, Yeşilkaya, Ediz, Ünay, Bülent

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Stevens-Johnson Syndrome triggered by a combination of clobazam, lamotrigine and valproic acid in a 7-year-old child von Yapici, A K, Fidanci, M K, Kilic, S, Balamtekin, N, Mutluay Arslan, M, Yavuz, S T, Kalman, S

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The effects of biotin supplementation on serum and liver tissue biotinidase enzyme activity and alopecia in rats which were administrated to valproic acid von Arslan, Mutluay, Vurucu, Sebahattin, Balamtekin, Necati, Unay, Bulent, Akin, Ridvan, Kurt, Ismail, Ozcan, Okan

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Ring chromosome 21 in the differential diagnosis of waddling gait von Arslan, Mutluay, Yiş, Uluç, Vurucu, Sebahattin, Tunca, Yusuf, Ünay, Bülent, Akin, Rıdvan

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Coexistence of severe developmental delay, epilepsy, and hemangioma in Snijders Blok‐Fisher syndrome suggests the presence of a POU3F3‐related SNIBFIS endophenotype: A case report... von Torun, Deniz, Arslan, Mutluay, Yüksel, Zafer

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Evaluation of resilience in pediatric well-controlled epilepsy patients von Arslan, Mutluay, Coşkun, Ayşe Nur, Üstün, Canan, Hür, Özgen, Ünay, Bülent

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De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome von Suls, Arvid, Jaehn, Johanna A., Kecskés, Angela, Weber, Yvonne, Weckhuysen, Sarah, Craiu, Dana C., Siekierska, Aleksandra, Djémié, Tania, Afrikanova, Tatiana, Gormley, Padhraig, von Spiczak, Sarah, Kluger, Gerhard, Iliescu, Catrinel M., Talvik, Tiina, Talvik, Inga, Meral, Cihan, Caglayan, Hande S., Giraldez, Beatriz G., Serratosa, José, Lemke, Johannes R., Hoffman-Zacharska, Dorota, Szczepanik, Elzbieta, Barisic, Nina, Komarek, Vladimir, Hjalgrim, Helle, Møller, Rikke S., Linnankivi, Tarja, Dimova, Petia, Striano, Pasquale, Zara, Federico, Marini, Carla, Guerrini, Renzo, Depienne, Christel, Baulac, Stéphanie, Kuhlenbäumer, Gregor, Crawford, Alexander D., Lehesjoki, Anna-Elina, de Witte, Peter A.M., Palotie, Aarno, Lerche, Holger, Esguerra, Camila V., De Jonghe, Peter, Helbig, Ingo, Hendrickx, Rik, Holmgren, Philip, Stephani, Ulrich, Muhle, Hiltrud, Pendiziwiat, Manuela, Appenzeller, Silke, Selmer, Kaja, Brilstra, Eva, Koeleman, Bobby, Rosenow, Felix, Leguern, Eric, Sterbova, Katalin, Magdalena, Budisteanu, Rodica, Gherghiceanu, Arsene, Oana Tarta, Diana, Barca, Guerrero-Lopez, Rosa, Ortega, Laura, Todorova, Albena P., Kirov, Andrey V., Robbiano, Angela, Arslan, Mutluay, Yiş, Uluç, Ivanović, Vanja

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A novel mutation in the sodium channel α1 subunit gene in a child with Dravet syndrome in Turkey von Arslan, Mutluay, Yiş, Uluç, Cağlayan, Hande, Akin, Rıdvan

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Basics of bone metabolism and osteoporosis in common pediatric neuromuscular disabilities von Yaşar, Evren, Adigüzel, Emre, Arslan, Mutluay, Matthews, Dennis J.

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Three Afghani siblings with a novel homozygous variant and further delineation of the clinical features of METTL5 related intellectual disability syndrome von Torun, Deniz, Arslan, Mutluay, Çavdarlı, Büşranur, Akar, Hatice, Cram, David Stephen

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Hypertrophic neuropathy of Sciatic nerve von Yiş, Uluç, Arslan, Mutluay, Güleryüz, Handan

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Autosomal recessive spinocerebellar ataxia 18 caused by homozygous exon 14 duplication in GRID2 and review of the literature von Ceylan, Ahmet Cevdet, Acar Arslan, Elif, Erdem, Haktan Bağış, Kavus, Haluk, Arslan, Mutluay, Topaloğlu, Haluk

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OP-128 Evaluation of interictal anxiety level and anxiety-related factors in children with epilepsy using anti-seizure drugs von Yılmaz, Buse, Coşkun, Ayşenur, Üstün, Canan, Arslan, Mutluay, ÜNAY, Bülent

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